| Tag | Content |
|---|
EnhancerAtlas ID | HS091-11181 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:122674920-122675920 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr12:122675644-122675661 | CAGGTCACTGTGACGTG | - | 6.09 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I122190 | chr12 | 122675541 | 122675690 |
|
Enhancer Sequence | GGTACTGGCA TGCAGGGAGG GGGTGGCATG TGACACCCCA GCCTGCGCCT GGCTGTGCCC 60
CGCCCTCCTG GGTCCGTGTA CCCGTCTGTC CTGCAACTCC CCATTTGACC CAGACCCTAT 120
TCAGGTATAG CCTCTCTTCT GGGTCAGAGC TTTCCACCAG GCTTTGATTC CTGTGATTGG 180
GATTTGGAGA CAGAAGTGAT AGGGGGAGGC CGGGCGCGGT GGCTAACGCC TGTAATCCCA 240
GCATTTTGGG AGGCTGAAGC AGACAGATCG CTTGAAGTCA GGAGTTTGAG ACCAGCCTGG 300
CCAACATGGT GAAACCTCGT CTGTACTAAA AATACAAAAA TTAGCCAGGC ATGGTGGCAA 360
GTGCCTGTAA TCCCAGCTAC TCAGGAGGCT GAGGCACGAG AATCTTTTGA ACCCGGGAGG 420
TGGAGGCTGC AGTGAGCCGA GATGACACCA GTGTACTCTA GCCTAGGTGA CAGAGCAAGA 480
CAAAAAAAAA AAAGGTGGTG TGGGAGGATC ACTTGAGCCC AGGAGGTGGA GGCTGCAGTG 540
AGCTATCATC TCACCACTGC ACTCTAGCCT GGCGACAGAG CGAGACCCCG TCTCTAAAAA 600
AAATAAAAAG TCAAAACAAC CTGTGGGGAC TTGGGACAGT TATTTCAATC AGCTTCTTCA 660
CCTCCCTGGT GGCTTGAGAT CACCCCCTTG TGGTTCATGC CGCAAGGTGC ACCGGAGGCT 720
TCTCCAGGTC ACTGTGACGT GCTAGATAAT GCTAAGGTGA CCTGCAGAGT AGCCCTTATC 780
ACTCCCATAT ACAGATCAGG AAAACAAGGC TGAAGAGGGG TATAATGACA CCTGGATCAC 840
TCCAGGCCAG CTTGCCAGAG CTGTGACATG AACCTGACCG CCCCACCAAG GCTCAGCCCT 900
GAGTGCTGGA GAGAATCTAG GGACCCGTGC CTTCCCAGCC CTCTTGCTTT CTATCTGCCA 960
ACTTCCATTC CATGGGCCCC CCTGTCCTGC CCATTCCTCC 1000
|
